D. A. Baylor

19.8k total citations · 7 hit papers
98 papers, 15.5k citations indexed

About

D. A. Baylor is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, D. A. Baylor has authored 98 papers receiving a total of 15.5k indexed citations (citations by other indexed papers that have themselves been cited), including 83 papers in Cellular and Molecular Neuroscience, 69 papers in Molecular Biology and 27 papers in Cognitive Neuroscience. Recurrent topics in D. A. Baylor's work include Photoreceptor and optogenetics research (60 papers), Retinal Development and Disorders (60 papers) and Neural dynamics and brain function (25 papers). D. A. Baylor is often cited by papers focused on Photoreceptor and optogenetics research (60 papers), Retinal Development and Disorders (60 papers) and Neural dynamics and brain function (25 papers). D. A. Baylor collaborates with scholars based in United States, Netherlands and Germany. D. A. Baylor's co-authors include King‐Wai Yau, Trevor D. Lamb, A. L. Hodgkin, Julie L. Schnapf, B J Nunn, Markus Meister, John G. Nicholls, M. G. F. Fuortes, Marie E. Burns and Fred Rieke and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

D. A. Baylor

96 papers receiving 14.6k citations

Hit Papers

Synchronous Bursts of Action Potentials in Ganglion ... 1968 2026 1987 2006 1991 1979 1971 1984 1968 250 500 750

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
D. A. Baylor United States 61 11.2k 10.8k 4.1k 924 841 98 15.5k
Peter Sterling United States 66 6.9k 0.6× 6.8k 0.6× 4.2k 1.0× 564 0.6× 678 0.8× 151 12.3k
Heinz Wässle Germany 83 14.4k 1.3× 16.2k 1.5× 3.8k 0.9× 2.3k 2.5× 488 0.6× 157 19.3k
Markus Meister United States 58 8.9k 0.8× 5.9k 0.6× 7.3k 1.8× 410 0.4× 2.0k 2.4× 93 15.2k
Carla J. Shatz United States 70 15.3k 1.4× 8.5k 0.8× 6.1k 1.5× 656 0.7× 896 1.1× 122 22.1k
R. W. Guillery United States 64 7.6k 0.7× 5.6k 0.5× 6.6k 1.6× 1.5k 1.6× 805 1.0× 149 13.9k
Edward N. Pugh United States 59 5.8k 0.5× 8.7k 0.8× 1.5k 0.4× 2.3k 2.5× 474 0.6× 180 12.1k
Fred Rieke United States 53 5.9k 0.5× 5.5k 0.5× 5.4k 1.3× 581 0.6× 454 0.5× 135 10.4k
Stephen W. Kuffler United States 43 7.2k 0.6× 5.0k 0.5× 3.2k 0.8× 274 0.3× 324 0.4× 53 11.0k
R. Llinás United States 81 14.8k 1.3× 8.8k 0.8× 9.2k 2.2× 373 0.4× 2.3k 2.8× 234 25.0k
Anita E. Hendrickson United States 59 5.7k 0.5× 7.6k 0.7× 4.8k 1.2× 4.4k 4.8× 721 0.9× 160 14.9k

Countries citing papers authored by D. A. Baylor

Since Specialization
Citations

This map shows the geographic impact of D. A. Baylor's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by D. A. Baylor with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites D. A. Baylor more than expected).

Fields of papers citing papers by D. A. Baylor

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D. A. Baylor. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by D. A. Baylor. The network helps show where D. A. Baylor may publish in the future.

Co-authorship network of co-authors of D. A. Baylor

This figure shows the co-authorship network connecting the top 25 collaborators of D. A. Baylor. A scholar is included among the top collaborators of D. A. Baylor based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with D. A. Baylor. D. A. Baylor is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Sampath, Alapakkam P. & D. A. Baylor. (2002). Molecular Mechanism of Spontaneous Pigment Activation in Retinal Cones. Biophysical Journal. 83(1). 184–193. 36 indexed citations
2.
Méndez, Ana, Marie E. Burns, Izabela Sokal, et al.. (2001). Role of guanylate cyclase-activating proteins (GCAPs) in setting the flash sensitivity of rod photoreceptors. Proceedings of the National Academy of Sciences. 98(17). 9948–9953. 214 indexed citations
3.
Burns, Marie E. & D. A. Baylor. (2001). Activation, Deactivation, and Adaptation in Vertebrate Photoreceptor Cells. Annual Review of Neuroscience. 24(1). 779–805. 311 indexed citations
4.
Rieke, Fred & D. A. Baylor. (2000). Origin and Functional Impact of Dark Noise in Retinal Cones. Neuron. 26(1). 181–186. 118 indexed citations
5.
Tsang, Stephen H., Marie E. Burns, Peter D. Calvert, et al.. (1998). Role for the Target Enzyme in Deactivation of Photoreceptor G Protein in Vivo. Science. 282(5386). 117–121. 170 indexed citations
6.
Rieke, Fred & D. A. Baylor. (1998). Origin of Reproducibility in the Responses of Retinal Rods to Single Photons. Biophysical Journal. 75(4). 1836–1857. 132 indexed citations
7.
Rieke, Fred & D. A. Baylor. (1998). Single-photon detection by rod cells of the retina. Reviews of Modern Physics. 70(3). 1027–1036. 156 indexed citations
8.
DeVries, Steven H. & D. A. Baylor. (1996). Correlated firing among different classes of ganglion cells in rabbit retina. Investigative Ophthalmology & Visual Science. 37(3). 3 indexed citations
9.
Baylor, D. A.. (1994). Introduction of King-Wai Yau 1993 Friedenwald Award winner.. PubMed. 35(1). 6–8. 1 indexed citations
10.
Meister, Markus, Jerome Pine, & D. A. Baylor. (1994). Multi-neuronal signals from the retina: acquisition and analysis. Journal of Neuroscience Methods. 51(1). 95–106. 327 indexed citations
11.
Zimmerman, Anita L. & D. A. Baylor. (1992). Cation interactions within the cyclic GMP‐activated channel of retinal rods from the tiger salamander.. The Journal of Physiology. 449(1). 759–783. 79 indexed citations
12.
Karpen, Jeffrey W., et al.. (1992). Cyclic GMP‐activated channels of salamander retinal rods: spatial distribution and variation of responsiveness.. The Journal of Physiology. 448(1). 257–274. 28 indexed citations
13.
Makino, Clint L., W. Rowland Taylor, & D. A. Baylor. (1991). Rapid charge movements and photosensitivity of visual pigments in salamander rods and cones.. The Journal of Physiology. 442(1). 761–780. 48 indexed citations
14.
Baylor, D. A.. (1989). CONDUCTANCE OF RETINAL PHOTORECEPTOR CELLS. 1 indexed citations
15.
Baylor, D. A. & B J Nunn. (1986). Electrical properties of the light‐sensitive conductance of rods of the salamander Ambystoma tigrinum.. The Journal of Physiology. 371(1). 115–145. 133 indexed citations
16.
Zimmerman, Anita L. & D. A. Baylor. (1986). Cyclic GMP-sensitive conductance of retinal rods consists of aqueous pores. Nature. 321(6065). 70–72. 269 indexed citations
17.
Zimmerman, Anita L., Gregory Yamanaka, F. Eckstein, D. A. Baylor, & Lubert Stryer. (1985). Interaction of hydrolysis-resistant analogs of cyclic GMP with the phosphodiesterase and light-sensitive channel of retinal rod outer segments.. Proceedings of the National Academy of Sciences. 82(24). 8813–8817. 157 indexed citations
18.
Baylor, D. A., B J Nunn, & Julie L. Schnapf. (1984). The photocurrent, noise and spectral sensitivity of rods of the monkey Macaca fascicularis.. The Journal of Physiology. 357(1). 575–607. 527 indexed citations breakdown →
19.
Baylor, D. A., T.D. Lamb, & King‐Wai Yau. (1979). The membrane current of single rod outer segments.. The Journal of Physiology. 288(1). 589–611. 244 indexed citations
20.
Baylor, D. A. & John G. Nicholls. (1969). Changes in extracellular potassium concentration produced by neuronal activity in the central nervous system of the leech. The Journal of Physiology. 203(3). 555–569. 176 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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